Ultrasound Guided Rectus Sheath Block for Pediatric Patients undergoing Abdominal Midline Operations: A randomized controlled trial.

Sixty patients of both sexes between 2 and 10 years old, ASA I ¿ II physical status, undergoing midline abdominal procedures are involved in this randomized controlled trial. Patients were randomly allocated into one of two groups (thirty patients each) ; group R (RSB group) and group C (control group). Both groups received general anesthesia . Group R received bilateral rectus sheath block with 0

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201505001103180

Enrollment

Registered

2015-04-16

Start date

2015-04-19

Completion date

Unknown

Last updated

2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Paediatrics surgery Anaesthesia

Interventions

group C

Group R

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: both sexes, ASA I ¿ II physical status, scheduled for elective abdominal midline operation.

Exclusion criteria

Exclusion criteria: Patients with hepatic disease, bleeding or neurological disorders, known hypersensitivity to local anesthetics, evidence of peritonitis, sepsis, or infection at the site of needle insertion and those who require emergency operations were excluded from the study.

Design outcomes

Primary

Measure	Time frame
The primary outcome measure was degree of pain according to Objective Bahavioral Pain scale.	—

Secondary

Measure	Time frame
secondary outcome measures were hemodynamic parameters, intraoperative fentanyl requirement and postoperative need for analgesia.	—

Countries

Egypt

Contacts

Public ContactMostafa Mansour

lecturer of anesthesia and intensive care

mostafa.mansor@med.asu.edu.eg+201093322145

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026